Canonical Allele Identifier: CA2676110949
Gene: GLRA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151851381_151851382insCTCGAGAGCC , CM000667.2:g.151851381_151851382insCTCGAGAGCC GRCh38
NC_000005.9:g.151230942_151230943insCTCGAGAGCC , CM000667.1:g.151230942_151230943insCTCGAGAGCC GRCh37
NC_000005.8:g.151211135_151211136insCTCGAGAGCC NCBI36
NG_011764.1:g.78455_78456insGGCTCTCGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.912+8_912+9insGGCTCTCGAG MANE Select ENSP00000274576.5:n.912+8_912+9insGGCTCTCGAG
ENST00000274576.8:c.912+8_912+9insGGCTCTCGAG ENSP00000274576.4:n.912+8_912+9insGGCTCTCGAG
ENST00000455880.2:c.912+8_912+9insGGCTCTCGAG ENSP00000411593.2:n.912+8_912+9insGGCTCTCGAG
ENST00000462581.6:c.*670+8_*670+9insGGCTCTCGAG ENSP00000430595.1:n.*670+8_*670+9insGGCTCTCGAG
ENST00000471351.2:n.1195+8_1195+9insGGCTCTCGAG
NM_000171.3:c.912+8_912+9insGGCTCTCGAG NP_000162.2:n.912+8_912+9insGGCTCTCGAG
NM_001146040.1:c.912+8_912+9insGGCTCTCGAG NP_001139512.1:n.912+8_912+9insGGCTCTCGAG
NM_001292000.1:c.663+8_663+9insGGCTCTCGAG NP_001278929.1:n.663+8_663+9insGGCTCTCGAG
XM_005268412.2:c.912+8_912+9insGGCTCTCGAG XP_005268469.1:n.912+8_912+9insGGCTCTCGAG
NM_000171.4:c.912+8_912+9insGGCTCTCGAG MANE Select NP_000162.2:n.912+8_912+9insGGCTCTCGAG
NM_001146040.2:c.912+8_912+9insGGCTCTCGAG NP_001139512.1:n.912+8_912+9insGGCTCTCGAG
NM_001292000.2:c.663+8_663+9insGGCTCTCGAG NP_001278929.1:n.663+8_663+9insGGCTCTCGAG